510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K132272Substantially Equivalent

Glooko Device System for Glooko Application

Glooko Inc, Palo Alto CA / Special, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K132272 is the FDA 510(k) clearance record for GLOOKO DEVICE SYSTEM FOR GLOOKO APPLICATION, a class II device, cleared for Glooko, Inc. on under FDA product code NBW (System, Test, Blood Glucose, Over The Counter). FDA records list 5 510(k) clearances for Glooko, Inc., from to . As of , FDA records show no recalls naming K132272.

Clearance record

Decision date
Received
(87 days to decision)
Product code
NBW System, Test, Blood Glucose, Over The Counter
Regulation
21 CFR 862.1345
Device class
Class II
Review panel
Clinical Chemistry
Applicant
Glooko, Inc. 170a University Ave., Palo Alto CA
510(k) summary
Summary PDF
Third party review
No

Clearances, product code NBW

Trailing 12 months
2 clearances under product code NBW in the twelve months to October 2026, July 2026 the highest month at 1.
Show the numbers
Monthly 510(k) clearances under FDA product code NBW, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20260
March 20260
April 20260
May 20260
June 20260
July 20261
August 20261
September 20260
October 20260